The following data is part of a premarket notification filed by Orthovita, Inc. with the FDA for Vitoss Scaffold Synthetic Cancellous Bone Void Filler.
| Device ID | K032409 |
| 510k Number | K032409 |
| Device Name: | VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER |
| Classification | Filler, Bone Void, Calcium Compound |
| Applicant | ORTHOVITA, INC. 45 GREAT VALLEY PKWY. Malvern, PA 19355 |
| Contact | Andreina Ide |
| Correspondent | Andreina Ide ORTHOVITA, INC. 45 GREAT VALLEY PKWY. Malvern, PA 19355 |
| Product Code | MQV |
| CFR Regulation Number | 888.3045 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-08-04 |
| Decision Date | 2003-08-29 |
| Summary: | summary |